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This book will cover topics related to the preparation and use of heterogeneous catalytic systems for the transformation of renewable sources, as well as of materials deriving from agro-industrial wastes and by-products. At the same time, the ever-increasing importance of bioproducts, due to the acceptance and request of consumers, makes the upgrade of biomass into chemicals and materials not only an environmental issue, but also an economical advantage.
isoselenourea --- malignant --- chemotherapeutics --- epigenetics --- antitumor activity --- methylseleninic acid --- mTOR inhibitors --- tumor heterogeneity --- hypoxia --- ER stress --- melanoma --- EMT --- lipid peroxidation --- immune evasion --- hypoxia-inducible factors (HIFs) --- selenium-binding protein 1 --- glutathione --- DNA damage --- hSP56 --- apoptosis --- tocopherol --- anticancer --- viability --- SELENBP1 --- selenium --- clear-cell renal cell carcinoma microRNAs --- SBP1 --- entosis --- PD-L1 --- miRNA --- cancer stem cells --- cell plasticity --- disease --- clear cell renal cell carcinoma --- HIF --- head and neck cancer --- selenium species --- VEGF --- STAT3 --- hypoxia-inducible factor --- methylselenocysteine --- anticancer agent --- Se-containing nanoparticles --- DNA damage and repair --- radiation --- seleno-l-methionine --- cancer --- tumor microenvironment --- methylselenoesters
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This book will cover topics related to the preparation and use of heterogeneous catalytic systems for the transformation of renewable sources, as well as of materials deriving from agro-industrial wastes and by-products. At the same time, the ever-increasing importance of bioproducts, due to the acceptance and request of consumers, makes the upgrade of biomass into chemicals and materials not only an environmental issue, but also an economical advantage.
isoselenourea --- malignant --- chemotherapeutics --- epigenetics --- antitumor activity --- methylseleninic acid --- mTOR inhibitors --- tumor heterogeneity --- hypoxia --- ER stress --- melanoma --- EMT --- lipid peroxidation --- immune evasion --- hypoxia-inducible factors (HIFs) --- selenium-binding protein 1 --- glutathione --- DNA damage --- hSP56 --- apoptosis --- tocopherol --- anticancer --- viability --- SELENBP1 --- selenium --- clear-cell renal cell carcinoma microRNAs --- SBP1 --- entosis --- PD-L1 --- miRNA --- cancer stem cells --- cell plasticity --- disease --- clear cell renal cell carcinoma --- HIF --- head and neck cancer --- selenium species --- VEGF --- STAT3 --- hypoxia-inducible factor --- methylselenocysteine --- anticancer agent --- Se-containing nanoparticles --- DNA damage and repair --- radiation --- seleno-l-methionine --- cancer --- tumor microenvironment --- methylselenoesters
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This book will cover topics related to the preparation and use of heterogeneous catalytic systems for the transformation of renewable sources, as well as of materials deriving from agro-industrial wastes and by-products. At the same time, the ever-increasing importance of bioproducts, due to the acceptance and request of consumers, makes the upgrade of biomass into chemicals and materials not only an environmental issue, but also an economical advantage.
isoselenourea --- malignant --- chemotherapeutics --- epigenetics --- antitumor activity --- methylseleninic acid --- mTOR inhibitors --- tumor heterogeneity --- hypoxia --- ER stress --- melanoma --- EMT --- lipid peroxidation --- immune evasion --- hypoxia-inducible factors (HIFs) --- selenium-binding protein 1 --- glutathione --- DNA damage --- hSP56 --- apoptosis --- tocopherol --- anticancer --- viability --- SELENBP1 --- selenium --- clear-cell renal cell carcinoma microRNAs --- SBP1 --- entosis --- PD-L1 --- miRNA --- cancer stem cells --- cell plasticity --- disease --- clear cell renal cell carcinoma --- HIF --- head and neck cancer --- selenium species --- VEGF --- STAT3 --- hypoxia-inducible factor --- methylselenocysteine --- anticancer agent --- Se-containing nanoparticles --- DNA damage and repair --- radiation --- seleno-l-methionine --- cancer --- tumor microenvironment --- methylselenoesters
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Despite the efficiency of current cancer treatments, cancer is still a deadly disease for too many. In 2008, 7.6 million people died of cancer; with the current development, it is estimated that the annual cancer death number will grow to 13 million by 2030. There is clearly a need for not only more research but also more innovative and out of the mainstream scientific ideas to discover and develop even better cancer treatments. This book presents the collective works published in the recent Special Issue entitled “Killing Cancer: Discovery and Selection of New Target Molecules”. These articles comprise a selection of studies, ideas, and opinions that aim to facilitate knowledge, thoughts, and discussion about which biological and molecular mechanisms in cancer we should target and how we should target them.
ferlin --- myoferlin --- dysferlin --- otoferlin --- C2 domain --- plasma membrane --- sulconazole --- NF-κB --- IL-8 --- mammosphere --- breast cancer stem cells --- AF1Q --- MLLT11 --- WNT --- STAT --- esophageal cancer --- prognosis --- mTORC1 --- mTORC2 --- metabolism --- rapalogs --- mTOR inhibitors --- cancer metabolism --- mTOR in immunotherapy --- nutrient metabolism --- kinase inhibitors --- mTOR signaling --- MAPK kinase --- ERK1 --- ERK2 --- CD domain --- Rolled --- SCH772984 --- VRT-11E --- sevenmaker --- cancer therapy --- EMT --- lysosome --- lysosome-mediated invasion --- MZF1 --- phosphorylation --- PAK4 --- SUMOylation --- transcription factor --- zinc finger --- glucocorticoids --- 3D growth --- nuclear factor kappa-light-chain-enhancer of activated B-cells (NF-κB) --- epithelial–mesenchymal transition --- anoikis --- proliferation --- targeted cancer therapy --- disulfiram --- NPL4 --- replication stress --- DNA damage --- BRCA1 --- BRCA2 --- ATR pathway --- PDAC --- TCIRG1 --- ATP6V0a3 --- invasion --- migration --- matrix degradation --- pH-regulation --- autophagy --- multidrug resistance in cancer --- drug efflux pumps --- ATP-binding cassette transporter --- breast cancer resistance protein (BCRP) --- ABCG2 --- pyrazolo-pyrimidine derivative --- SCO-201 --- colorectal cancer --- immunotherapy --- inflammation --- microsatellite instability --- oncofetal chondroitin sulfate --- chondroitin sulfate --- cancer --- solid tumors --- target --- pediatric cancer --- VAR2 --- dexamethasone --- thyroid cancer --- microgravity --- space environment --- n/a --- epithelial-mesenchymal transition
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Despite the efficiency of current cancer treatments, cancer is still a deadly disease for too many. In 2008, 7.6 million people died of cancer; with the current development, it is estimated that the annual cancer death number will grow to 13 million by 2030. There is clearly a need for not only more research but also more innovative and out of the mainstream scientific ideas to discover and develop even better cancer treatments. This book presents the collective works published in the recent Special Issue entitled “Killing Cancer: Discovery and Selection of New Target Molecules”. These articles comprise a selection of studies, ideas, and opinions that aim to facilitate knowledge, thoughts, and discussion about which biological and molecular mechanisms in cancer we should target and how we should target them.
Research & information: general --- Biology, life sciences --- ferlin --- myoferlin --- dysferlin --- otoferlin --- C2 domain --- plasma membrane --- sulconazole --- NF-κB --- IL-8 --- mammosphere --- breast cancer stem cells --- AF1Q --- MLLT11 --- WNT --- STAT --- esophageal cancer --- prognosis --- mTORC1 --- mTORC2 --- metabolism --- rapalogs --- mTOR inhibitors --- cancer metabolism --- mTOR in immunotherapy --- nutrient metabolism --- kinase inhibitors --- mTOR signaling --- MAPK kinase --- ERK1 --- ERK2 --- CD domain --- Rolled --- SCH772984 --- VRT-11E --- sevenmaker --- cancer therapy --- EMT --- lysosome --- lysosome-mediated invasion --- MZF1 --- phosphorylation --- PAK4 --- SUMOylation --- transcription factor --- zinc finger --- glucocorticoids --- 3D growth --- nuclear factor kappa-light-chain-enhancer of activated B-cells (NF-κB) --- epithelial-mesenchymal transition --- anoikis --- proliferation --- targeted cancer therapy --- disulfiram --- NPL4 --- replication stress --- DNA damage --- BRCA1 --- BRCA2 --- ATR pathway --- PDAC --- TCIRG1 --- ATP6V0a3 --- invasion --- migration --- matrix degradation --- pH-regulation --- autophagy --- multidrug resistance in cancer --- drug efflux pumps --- ATP-binding cassette transporter --- breast cancer resistance protein (BCRP) --- ABCG2 --- pyrazolo-pyrimidine derivative --- SCO-201 --- colorectal cancer --- immunotherapy --- inflammation --- microsatellite instability --- oncofetal chondroitin sulfate --- chondroitin sulfate --- cancer --- solid tumors --- target --- pediatric cancer --- VAR2 --- dexamethasone --- thyroid cancer --- microgravity --- space environment
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The mechanistic target of rapamycin (mTOR) is a major signaling intermediary that coordinates favorable environmental conditions with cell growth. Indeed, as part of two functionally distinct protein complexes, named mTORC1 and mTORC2, mTOR regulates a variety of cellular processes, including protein, lipid, and nucleotide synthesis, as well as autophagy. Over the last two decades, major molecular advances have been made in mTOR signaling and have revealed the complexity of the events implicated in mTOR function and regulation. In parallel, the role of mTOR in diverse pathological conditions has also been identified, including in cancer, hamartoma, neurological, and metabolic diseases. Through a series of articles, this book focuses on the role played by mTOR in cellular processes, metabolism in particular, and highlights a panel of human diseases for which mTOR inhibition provides or might provide benefits. It also addresses future studies needed to further characterize the role of mTOR in selected disorders, which will help design novel therapeutic approaches. It is therefore intended for everyone who has an interest in mTOR biology and its application in human pathologies.
n/a --- primary cilia --- neurodegeneration --- nutrient sensor --- PI3K --- transcriptomics --- phosphorylation --- metabolic reprogramming --- autophagy --- Alzheimer’s disease --- rapalogs --- liver --- angiogenesis --- mTOR complex --- MBSCs --- advanced biliary tract cancers --- Medulloblastoma --- epithelial to mesenchymal transition --- AMPK --- p70S6K --- lipid metabolism --- thyroid cancer --- sodium iodide symporter (NIS)/SLC5A5 --- male fertility --- anesthesia --- illumina --- mTOR inhibitor --- miRNA --- Hutchinson-Gilford progeria syndrome (HGPS) --- eIFs --- Emery-Dreifuss muscular dystrophy (EDMD) --- glucose --- AKT --- oral cavity squamous cell carcinoma (OSCC) --- glucose and lipid metabolism --- cellular signaling --- aging --- tumor microenvironment --- rapamycin --- leukemia --- chloral hydrate --- rapalogues --- schizophrenia --- T-cell acute lymphoblastic leukemia --- senescence --- lamin A/C --- neurotoxicity --- neurodevelopment --- inhibitor --- methamphetamine --- pulmonary fibrosis --- mTOR --- mTOR inhibitors --- combination therapy --- proteolysis --- fluid shear stress --- tumour cachexia --- biomarkers --- synapse --- gluconeogenesis --- mTOR signal pathway --- Sertoli cells --- immunosenescence --- miRNome --- protein aggregation --- senolytics --- metabolism --- NGS --- mTORC2 --- mTORC1 --- metabolic diseases --- IonTorrent --- apoptosis --- dopamine receptor --- nocodazole --- microenvironment --- everolimus --- acute myeloid leukemia --- immunotherapy --- spermatogenesis --- bone remodeling --- signalling --- targeted therapy --- ageing --- therapy --- NVP-BEZ235 --- fructose --- physical activity --- laminopathies --- MC3T3-E1 cells --- cell signaling --- microRNA --- cancer --- lipolysis --- melatonin --- Parkinson’s disease --- Alzheimer's disease --- Parkinson's disease
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Renal cancer is a health problem of major concern worldwide. Although tyrosine kinase inhibitors and immune check-point blockade treatments, alone or in combination, are giving promising results, failures are quite frequent due to intratumor heterogeneity and to the acquisition of drug resistance. The spectrum of renal cell carcinoma subtypes is wide. Up to 70–80% of renal tumors are clear cell renal cell carcinomas, a clinically aggressive tumor subtype linked to VHL gene inactivation. Next in frequency, the papillary renal cell carcinoma category encompasses an intricate puzzle of classic and newly described entities with poorly defined limits, some of them pending definite clarification. Likewise, the chromophobe–oncocytoma duality, the so-called hybrid tumors and oncocytic neoplasms, remain to be well profiled. Finally, a growing list of very uncommon renal tumors linked to specific molecular signatures fulfill the current portrait of renal cell neoplasia. This Special Issue of Cancers regards RCC from very different perspectives, from the intimate basic mechanisms governing this disease to the clinical practice principles of their diagnoses and treatments. The interested reader will have the opportunity to contact with some of the most recent findings and will be updated with excellent reviews.
Renal cell carcinoma. --- Kidneys --- Cancer. --- Adenocarcinoma of kidney --- Clear cell carcinoma --- Grawitz tumor --- Grawitz's tumor --- Hypernephroid carcinoma --- Hypernephroma --- Renal adenocarcinoma --- Renal cell adenocarcinoma --- Cancer --- N-glycomapping --- n/a --- SMAD proteins --- patient survival --- pro-IL-1? --- survival prediction --- inflammation markers --- tumor migration --- prognostic factors --- practical approach --- circular RNAs in a clinico-genomic predictive model --- glycomarkers --- review --- nephrectomy --- uric acid --- VEGF inhibitors --- metabolic reprogramming --- collecting duct carcinoma --- curcumin --- metabolome profiling --- identification of circular RNAs --- IL-2 --- experimental validation of circular RNA --- Raf/MEK/ERK --- HOT --- PI3K/Akt/mTOR --- pentose phosphate pathway --- kidney cancer --- LOT --- mutation --- RCC --- polybromo-1 --- pale cell --- MMP-9 --- gene expression --- recurrence free survival --- chromosomal loss --- IL-1? --- chronic kidney disease --- glutathione transferase omega 2 --- label-free --- glutathione transferase omega 1 --- emerging entity --- copy number alteration --- FOXO3 --- predictive role --- tumor slice culture --- tyrosine kinase inhibitors --- PPP --- ESC --- CDKN1A expression --- metastasis --- PD-L1 --- diagnostic and prognostic markers --- EVI1 --- copy number loss --- RNA sequencing --- NK cells --- glutathione metabolism --- clear cell renal cell carcinoma --- renal cell cancer --- proliferation --- eosinophilic variant --- Xp11 translocation renal cell carcinoma --- prognosis --- invasion --- immune infiltration --- IL4R? --- FISH --- 11) translocation renal cell carcinoma --- tumor microenvironment --- metabolome --- hyperosmolality --- toxicity --- ALK --- drug sensitivity --- t(6 --- copy number analysis --- urine --- genetic association --- polymorphism --- solute carrier proteins --- kidney --- metastatic ccRCC --- molecular genetic features --- recurrence-free survival --- chromophobe renal cell carcinoma --- unclassified renal tumor --- overall survival --- mTOR inhibitors --- mTOR --- JAK2 --- von Hippel–Lindau --- miR-155-5p --- glycoproteomics --- PBRM1 --- miR-133b --- survival --- TFE3 --- TFEB --- oncocytic renal tumor --- immune checkpoint inhibitors --- biomarker --- MMP10 --- TCGA --- ghrelin --- EMT like --- checkpoint inhibitors --- MiT family translocation renal cell carcinoma --- gene signature --- sarcomatoid --- transforming growth factor beta --- clear cell Renal Cell Carcinoma --- tumor adhesion --- renal cancer --- unclassified renal cell carcinoma --- Papillary renal cell carcinoma (pRCC) --- miR-146a-5p --- renal cell --- everolimus --- integrins --- cytoreductive nephrectomy --- immunotherapy --- predictive factors --- immunohistochemistry --- MTA2 --- IL13R?1 --- targeted therapy --- intratumour heterogeneity --- aurora A --- TCA cycle --- AMP-activated protein kinases --- cancer-specific survival --- programmed death-ligand 1 --- efficacy --- renal cell carcinoma --- anaplastic lymphoma kinase rearrangement --- TFEB-amplified renal cell carcinoma --- statins --- cancer immunotherapy --- microRNA --- new entity --- proteome profiling --- von Hippel-Lindau
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